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Efficacy and Safety Study of LE-DT to Treat Metastatic Castrate Resistant Prostate Cancer

2018年3月8日 更新者:INSYS Therapeutics Inc

A Multicenter, Open-Label, Phase II Study of LE-DT for Efficacy and Safety in Patients With Metastatic Castrate Resistant Prostate Cancer

LE-DT is a novel, proprietary delivery system of docetaxel developed by NeoPharm, Inc. Docetaxel (currently marketed as Taxotere) is an anti-microtubular network agent and is one of the most active agents in the treatment of metastatic castrate resistant prostate cancer (CRPC) and other variety of cancers. Taxotere has poor solubility and is designed to be administered with Tween 80 in ethanol. This vehicle causes acute hypersensitivity reaction. By removing toxic detergent used in Taxotere, the form of LE-DT, shows reduced toxicity and comparable therapeutic efficacy in pre-clinical study. The clinical evidence obtained from the NeoPharm Phase I study shows fewer side effects and possibly administered at higher dose to induce greater effectiveness of LE-DT. The current Phase II study is designed to accomplish the following objectives:

  1. Assess the antitumor effect indicator serum prostate specific antigen (PSA) following the intravenous (IV) administration of 110 mg/m2 LE-DT every three weeks in patients with metastatic castrate resistant prostate cancer
  2. To evaluate the measurable soft tissue disease response using the response evaluation criteria in solid tumor (RECIST) methodology
  3. To evaluate the progression-free survival (PFS) and overall survival (OS)
  4. To correlate PSA expression with tumor response
  5. To evaluate the safety of LE-DT at 110 mg/m2 level, in particular peripheral neuropathy, water retention as well as myelotoxicity
  6. To evaluate the quality of life (QOL)

調査の概要

状態

引きこもった

研究の種類

介入

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • District of Columbia
      • Washington、District of Columbia、アメリカ、20007
        • Georgetown University Medical Center
    • Oregon
      • Portland、Oregon、アメリカ、97213-2933
        • Providence Portland Medical Center

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

説明

Inclusion Criteria:

  1. Be 18 years or older and male.
  2. Have histologically or cytologically confirmed diagnosis of adenocarcinoma of the prostate.
  3. Patients without evidence of PSA progression must have clinical or radiographic evidence of metastatic disease.
  4. Must have castrate levels of testosterone (serum testosterone less than 50ng/dl) by either being on androgen ablation therapy with a luteinizing hormone-releasing hormone (LHRH) agonist or have had a prior bilateral orchiectomy.
  5. Patients must have documented evidence of disease progression: progressive disease is defined as a minimum of three consecutive elevations in PSA each obtained a minimum of one week apart with the last value being greater than 2 ng/mL and/or new metastatic lesions on bone scan (minimum of 2) and/or new or progressive disease on CT or MRI scan.
  6. For patients on an antiandrogen (flutamide, nilutamide, bicalutamide)

    1. If given as part of first line therapy or for patients who did respond to antiandrogen second line therapy, the patient must demonstrate progression of disease at least 4 weeks beyond discontinuation of such agents to rule out an antiandrogen withdrawal response.
    2. If given as a second line therapy and the patient did not respond or had a decline in PSA for less than 3 months, it is not required to observe for a withdrawal response.
  7. Chemotherapy-naïve patients (unlimited prior regimens of hormonal therapy are acceptable).
  8. Have no other malignancy within the past five years, except non-melanoma, skin cancer.
  9. Have recovered from acute toxicities of prior treatment:

    1. Greater than or equal to 4 weeks must have elapsed since receiving hormonal therapy (except for chronic non-investigational gonadotropin releasing hormone analogs or other primary androgen suppressive therapy which are required), biologic agents or any investigational agent (palliative bisphosphonate therapy for bone pain can be administered as clinically indicated).
    2. Greater than or equal to 4 weeks must have elapsed since receiving any radiotherapy
    3. Greater than or equal to 2 weeks must have elapsed since any prior surgery or granulocyte-stimulating growth factor therapy.
  10. Have the following hematology levels at Baseline:

    1. Absolute Neutrophil Count (ANC) greater than or equal to1,500 x 106 cells/L
    2. Platelets greater than or equal to 100 x 109 cells/L
    3. Hemoglobin greater than or equal to 9 g/L.
  11. Have the following chemistry levels at Baseline:

    1. AST (SGOT), ALT (SGPT) less than or equal to 1.5 x ULN
    2. Total bilirubin less than or equal to 1.5 ULN
    3. Creatinine less than or equal to 1.5 ULN; or 24-hour creatinine clearance greater than 60 mL/min
    4. Normal serum electrolytes and magnesium levels
  12. Have a life expectancy of greater than or equal to 12 weeks.
  13. Have an Eastern Cooperative Oncology Group (ECOG) Performance status of 0-2.
  14. Patient or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee (EC)/Institutional Review Board (IRB)-approved written informed consent form (ICF) prior to receiving any study related procedure.

Exclusion Criteria:

  1. Patient has radiographic evidence of active (symptomatic, untreated) intraparenchymal brain metastases; any meningeal metastases; or asymptomatic untreated intraparenchymal brain metastases requiring treatment.
  2. Patient has received prior chemotherapy for metastatic prostate cancer.
  3. Patient has a known infection with human immunodeficiency virus or active viral hepatitis.
  4. Patient has active heart disease including myocardial infarction or congestive heart failure within the previous 6 months, symptomatic coronary artery disease, or uncontrolled arrhythmias.
  5. Any condition which in the Investigator's opinion deems the patient an unsuitable candidate to receive study drug (e.g., uncontrolled bleeding or bleeding diathesis).
  6. Any active infection requiring parenteral or oral antibiotics.
  7. Patient treated with any of the following:

    1. Taxol, Taxotere or Abraxane for prostate cancer or any prior malignancy
    2. Concurrent radiation therapy (except for palliative radiotherapy for symptomatic bone metastasis which can be administered as clinically indicated)
  8. Patient has pre-existing peripheral neuropathy of Grade greater than 1 based on the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE).

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Liposome Entrapped Docetaxel (LE-DT)
Disease status and tumor responses/progression is assessed in accordance to the RECIST guideline
110 mg/m2 IV (in vein) on day 1 of each 21 day cycle, 6 cycles or until disease progression or unacceptable toxicity
他の名前:
  • LE-DT
  • リポソーム ドセタキセル

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Assessment of serum PSA
時間枠:1 year
Measure serum PSA after 2, 4 and 6 cycles of treatment
1 year

二次結果の測定

結果測定
メジャーの説明
時間枠
RECIST method assessment
時間枠:1 year
Measurable soft tissue disease response based on the RECIST method, PFS, and OS will also be assessed after 2, 4 and 6 cycle to determine the treatment effectiveness with LE-DT after treatment
1 year

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Nancy A Dawson, M.D.、Georgetown University
  • 主任研究者:Brendan D Curti, M.D.、Providence Health & Services

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2010年6月1日

一次修了 (予想される)

2011年9月1日

研究の完了 (予想される)

2011年9月1日

試験登録日

最初に提出

2010年8月19日

QC基準を満たした最初の提出物

2010年8月23日

最初の投稿 (見積もり)

2010年8月25日

学習記録の更新

投稿された最後の更新 (実際)

2018年3月12日

QC基準を満たした最後の更新が送信されました

2018年3月8日

最終確認日

2018年3月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

前立腺がんの臨床試験

  • Jonsson Comprehensive Cancer Center
    National Cancer Institute (NCI); Highlight Therapeutics
    積極的、募集していない
    平滑筋肉腫 | 悪性末梢神経鞘腫瘍 | 滑膜肉腫 | 未分化多形肉腫 | 骨の未分化高悪性度多形肉腫 | 粘液線維肉腫 | II期の体幹および四肢の軟部肉腫 AJCC v8 | III期の体幹および四肢の軟部肉腫 AJCC v8 | IIIA 期の体幹および四肢の軟部肉腫 AJCC v8 | IIIB 期の体幹および四肢の軟部肉腫 AJCC v8 | 切除可能な軟部肉腫 | 多形性横紋筋肉腫 | 切除可能な脱分化型脂肪肉腫 | 切除可能な未分化多形肉腫 | 軟部組織線維肉腫 | 紡錘細胞肉腫 | ステージ I 後腹膜肉腫 AJCC (American Joint Committee on Cancer) v8 | 体幹および四肢の I 期軟部肉腫 AJCC v8 | ステージ... およびその他の条件
    アメリカ

Liposome Entrapped Docetaxel (LE-DT)の臨床試験

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